非酶糖基化和加热对人角质层和指甲褐变的影响。

Dermatologica Pub Date : 1991-01-01 DOI:10.1159/000247669
H Sueki, S Nozaki, S Numazawa, K Aoki, Y Kuroiwa, R Fujisawa
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引用次数: 7

摘要

本研究的目的是探讨非酶糖基化和随后的加热对足底角质层和指甲褐变的影响,并阐明糖尿病患者黄皮肤和黄指甲的发病机制。我们将非糖尿病患者的角质层和指甲分别在0(对照)、10(仅指甲)、20(仅指甲)、100和250 mM葡萄糖缓冲液中37℃孵育5天。糖基化后的样品在蒸馏水下透析96 h,每24 h换一次蒸馏水,然后干燥24 h,用糠氨酸含量测定非酶糖基化程度。每5mg样品用6n盐酸水解,用高效液相色谱法测定糠氨酸。每个样品的其余部分分别在37、42(仅钉子)、47和52℃下保存14天。肉眼观察角质层褐变情况,分光光度法观察指甲褐变情况。根据它们的分光光度反射率。计算Munsell评分(H =色相评分,V =亮度评分,C =饱和度评分)和(H + C)/V,客观评价褐变。与葡萄糖缓冲液孵育角质层和指甲增加其非酶糖基化(糠氨酸)剂量依赖。宏观上看,角质层褐变与葡萄糖浓度和贮藏温度成正比。然而,样品在10和20毫米葡萄糖中孵育,并在42℃下储存,没有显示出明显的褐变。经过糖基化和加热处理的指甲样品的Munsell评分显示色调和饱和度增加,但亮度降低。指甲样品的(H + C)/V值显著高于对照组。我们无法在棕色样品中检测到任何荧光。体外实验表明,角质层和指甲的褐变取决于非酶糖基化的程度和储存温度。我们提出了一种假设,即非酶糖基化和角质层和指甲的储存温度可能是糖尿病患者黄皮肤和黄指甲发生的一个因素。
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Effect of non-enzymatic glycosylation and heating on browning of human stratum corneum and nail.

The purpose of the present study was to examine the effect of non-enzymatic glycosylation and subsequent heating on the browning of the plantar stratum corneum and the finger-nail, and to elucidate the pathogenesis of the yellow skin and the yellow nail seen in diabetic subjects. We incubated stratum corneum and nail from non-diabetics in 0 (control), 10 (only nail), 20 (only nail), 100 and 250 mM glucose buffer at 37 degrees C for 5 days. These glycosylated samples were dialysed against distilled water for 96 h. Distilled water was changed every 24 h. Then samples were dried for 24 h. The extent of non-enzymatic glycosylation was measured by furosine content. Each 5 mg of sample was hydrolysed by 6 N HCl and processed for measurement of furosine by high-performance liquid chromatography. The rest of each sample was stored at 37, 42 (only nail), 47 and 52 degrees C for 14 days. Browning of the stratum corneum was assessed macroscopically, and that of the nail by spectrophotometry. Based on their spectrophotometric reflectances. Munsell's scores (H = hue score, V = lightness score, C = saturation score) and (H + C)/V were calculated for objective evaluation of browning. Incubation of the stratum corneum and nail with glucose buffer increased their non-enzymatic glycosylation (furosine) dose dependently. Macroscopically, the browning of the stratum corneum was enhanced in proportion to the glucose concentration and storage temperature. However, samples incubated in 10 and 20 mM glucose and stored at 42 degrees C did not show visible browning. Munsell's score of the nail samples treated by glycosylation and heating showed increased hue and saturation but reduced lightness. (H + C)/V values of these nail samples were significantly higher than those of the control. We could not detect any fluorescence with Wood light in the browned samples. The present in vitro study demonstrated that the browning of the stratum corneum and the nail depended on the extent of both non-enzymatic glycosylation and storage temperature. We suggested a hypothesis that the non-enzymatic glycosylation and the storage temperature of the stratum corneum and the nail might be a contributory factor in the development of yellow skin and yellow nail in diabetic patients.

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